In reply to today's poll (27 Nov 11), I asked:
45% (current count) use 2 other forums, and 63% use 2 or 3. This is the only one I've been using (joined not long ago). What are some of those other PD forums that others also use?
In reply to today's poll (27 Nov 11), I asked:
45% (current count) use 2 other forums, and 63% use 2 or 3. This is the only one I've been using (joined not long ago). What are some of those other PD forums that others also use?
I am a constant visitor and supporter of the Michael J Fox foundation.
Thanks, larry. It looks like that's a good single source for info about PD. I've been living with and seeing neurologists about PD, but I really should be learning and doing more about it. That site will help with that (I've added it to my home page set).
Thanks, Beachdog. I've been to parkinson.org before, but I'll add it to my list/bookmarks now. It's time for me to get more organized about this. I'll check out the other one too, even though it was ~2 years since I was diagnosed.
Clarification:
When I said:
> I've been living with and seeing neurologists about PD,
I didn't mean that I've been living with neurologists and seeing neurologists about PD. I meant I've been living with PD and seeing neurologists about PD.
i also go to the micHeal j fox site a lot but have just registered with parkinsonsuk site too - but hae to say that this is the BEST -